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Field Intervention Specialist; Cath lab-REMOTE- travel

Remote / Online - Candidates ideally in
Scottsdale, Maricopa County, Arizona, 85250, USA
Listing for: Teleflex Incorporated
Full Time, Remote/Work from Home position Listed on 2026-11-05
Job specializations:
  • Healthcare
    Clinical Research, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 120000 - 126000 USD Yearly USD 120000.00 126000.00 YEAR

Job Description & How to Apply Below

Position: Field Intervention Specialist (Cath lab-REMOTE- 70% travel)

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Field Intervention Specialist (Cath lab-REMOTE- 70% travel)

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.

Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, Quik Clot™, Rüsch™, Uro Lift™ and Weck™ – trusted brands united by a common sense of purpose.

At Teleflex, we are empowering the future of healthcare. For more information, please visit .

Interventional – The Interventional business unit at Teleflex develops innovative medical devices used to diagnose and treat coronary and peripheral vascular diseases. We focus strategically on coronary and peripheral interventions, vascular and bone access, and large-bore closure solutions.

Our portfolio includes a broad range of clinically relevant products, such as the Guide Liner™ and Turnpike™ Catheters; the Orsiro™ Mission™ Drug-Eluting Stent; the PK Papyrus™ Covered Coronary Stent; the Ringer™ Perfusion Balloon Catheter; the Pulsar™
-18 T3 Self-Expanding Stent;
Passeo™ Balloon Catheters; and the OnControl™ Powered Bone Access System.

Backed by a strong R&D pipeline, our rapidly growing Interventional business unit is well positioned to continue advancing new technologies that support the treatment of critically ill patients. Join a dynamic team dedicated to delivering innovative medical solutions that make a meaningful difference in patients’ lives.

Position Summary
  • Establish and maintain clinical trial sites for interventional cardiology studies (coronary and peripheral).
  • Train site personnel and investigators on study devices and clinical protocols.
  • Provide technical and clinical support during device implants and follow-ups.
  • Serve as a resource for site coordinators, investigators, and field personnel.
  • Ensure accurate and complete data collection in compliance with study protocols.
  • Assist in timely data collection and submission to meet protocol requirements.
  • Develop and maintain professional relationships with investigators and sites.
  • Identify, elevate, and resolve logistical and operational issues during study execution.
  • Report and address serious protocol compliance issues.
  • Support onboarding and training of newly hired specialists, as needed.
  • Support quality improvement initiatives.
  • Contribute to process and procedure enhancements under the direction of clinical management.
Education / Experience Requirements
  • Bachelor’s degree in a health, science, or engineering field preferred. Candidates with an Associate degree may be considered with 3+ years of directly relevant experience.
  • Minimum of three years’ experience supporting clinical studies on behalf of industry in the field of vascular intervention, preferably peripheral or cardiac stents.
  • Minimum of three years’ clinical experience in the Cardiac Catheterization Lab is required.
Specialized Skills / Other Requirements
  • Experience with one or more phases of clinical studies (start-up, management, closure), either with Teleflex or another company.
  • Ability to manage multiple projects concurrently.
  • Strong working knowledge and understanding of FDA, ICH, and GCP regulations governing clinical trials, standard regulatory and clinical practices, and current regulatory issues related to clinical research.
  • Additional experience in clinical settings, biostatistics, IDE clinical…
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